59464-15-2 Usage
Description
1-(2-amino-6-oxo-1,6-dihydropyrimidin-5-yl)-1,4-anhydropentitol is a complex chemical compound characterized by the presence of a dihydropyrimidine ring with an amino group and a ketone group, as well as a pentitol ring with an anhydride group. This unique structure suggests potential applications in various fields, particularly in pharmaceuticals, due to the biological activity often associated with dihydropyrimidine-containing molecules. The anhydride group also indicates possible utility in organic synthesis reactions. However, further research is necessary to fully comprehend the properties and potential uses of this compound.
Uses
Used in Pharmaceutical Industry:
1-(2-amino-6-oxo-1,6-dihydropyrimidin-5-yl)-1,4-anhydropentitol is used as a potential pharmaceutical compound for its possible incorporation into biologically active molecules. The presence of the dihydropyrimidine ring, which is common in various pharmaceutical agents, suggests that this compound could be a valuable building block for the development of new drugs.
Used in Organic Synthesis:
1-(2-amino-6-oxo-1,6-dihydropyrimidin-5-yl)-1,4-anhydropentitol is used as a synthetic building block for its anhydride group, which could be exploited in organic synthesis reactions to create a variety of complex molecules with potential applications in different industries, including pharmaceuticals, materials science, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 59464-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,4,6 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59464-15:
(7*5)+(6*9)+(5*4)+(4*6)+(3*4)+(2*1)+(1*5)=152
152 % 10 = 2
So 59464-15-2 is a valid CAS Registry Number.
59464-15-2Relevant articles and documents
A stereocontrolled total synthesis of C-nucleosides
Sato,Hayakawa,Noyori
, p. 2515 - 2525 (2007/10/02)
A stereocontrolled, general synthesis of chiral C-nucleosides has been achieved through a common lactonic C- beta -glycoside intermediate which is readily obtainable from non-carbohydrate materials. The optically pure lactone having the natural D configuration is obtained through optical resolution of the seco acid by the Pirkle's method followed by relactonization. alpha -Aminomethylenation of the lactone with t-C//4H//9OCH left bracket N(CH//3 )//2 right bracket //2 yields 2-(2,3-0-isopropylidene- beta -D-ribofuranosyl)-2-(dimethylaminomethylene)acetic acid lactone, which undergoes base-assisted condensation with urea followed by deprotection to furnish naturally occurring pseudouridine. Analogously, construction of heterocycles using thiourea and guanidine converts the aminomethylene lactone to unnatural pyrimidine C-nucelosides, 2-thiopseudouridine and pseudoisocytidine, respectively.
